aMAP Score and Its Combination With Liver Stiffness Measurement Accurately Assess Liver Fibrosis in Chronic Hepatitis

Rong Fan1, Guanlin Li2, Ning Yu1

  • 1Guangdong Provincial Key Laboratory of Viral Hepatitis Research, Guangdong Provincial Clinical Research Center for Viral Hepatitis, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China.

Abstract

Insights

The age-male-albumin-bilirubin-platelets (aMAP) score shows promise for diagnosing liver fibrosis in chronic hepatitis B (CHB) patients. A new aMAP-LSM model accurately assesses fibrosis stage, especially after treatment.

Area of Science:

  • Hepatology
  • Gastroenterology
  • Medical Diagnostics

Background:

  • Liver stiffness measurement (LSM) is unreliable for tracking fibrosis regression in treated chronic hepatitis B (CHB) patients.
  • The age-male-albumin-bilirubin-platelets (aMAP) score, a known hepatocellular carcinoma risk predictor, may indicate liver fibrosis.
  • Accurate noninvasive methods are needed to assess liver fibrosis in CHB patients, both treated and untreated.

Purpose of the Study:

  • To evaluate the diagnostic performance of the aMAP score for liver fibrosis in CHB patients.
  • To assess the utility of aMAP in conjunction with LSM for fibrosis staging.
  • To develop and validate a novel model for estimating fibrosis stage in treated CHB patients.

Main Methods:

  • Cross-sectional analysis of 2053 CHB patients from real-world and clinical trial data.
  • Longitudinal analysis of 889 CHB patients with paired liver biopsies before and after antiviral treatment (72 or 104 weeks).
  • Evaluation of aMAP score, LSM, and a combined aMAP-LSM model for diagnosing cirrhosis and advanced fibrosis.

Main Results:

  • The aMAP score demonstrated good performance in diagnosing cirrhosis (AUC 0.788) and advanced fibrosis (AUC 0.757).
  • Combining aMAP and LSM improved diagnostic accuracy and reduced uncertainty for cirrhosis (82.3%) and advanced fibrosis (79.8%).
  • The novel aMAP-LSM model showed high accuracy in diagnosing fibrosis post-treatment (AUC 0.839 for cirrhosis, 0.840 for advanced fibrosis), outperforming LSM alone.

Conclusions:

  • The aMAP score is a valuable noninvasive tool for diagnosing liver fibrosis in CHB patients.
  • The aMAP-LSM model offers accurate fibrosis staging for treated CHB patients, particularly when LSM shows significant improvement.
  • These findings support the use of aMAP-based approaches for noninvasive liver fibrosis assessment in CHB.